|
HS Code |
887385 |
| Product Name | 3-Bromo-5-Hydroxymethylpyridine |
| Cas Number | 63500-71-0 |
| Molecular Formula | C6H6BrNO |
| Molecular Weight | 188.02 |
| Appearance | White to off-white solid |
| Purity | Typically ≥ 98% |
| Melting Point | 56-60°C |
| Solubility | Soluble in organic solvents like DMSO and ethanol |
| Synonyms | 3-Bromo-5-(hydroxymethyl)pyridine |
| Smiles | C1=CC(=CN=C1CBr)CO |
| Inchi | InChI=1S/C6H6BrNO/c7-6-2-5(3-9)1-4-8-6/h1-2,4,9H,3H2 |
| Storage Temperature | 2-8°C (Refrigerated) |
| Hazard Class | Irritant |
As an accredited 3-Bromo-5-Hydroxymethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3-Bromo-5-Hydroxymethylpyridine is supplied in a sealed, amber glass bottle with tamper-evident cap and labeled with hazard information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-Bromo-5-Hydroxymethylpyridine: Loaded securely in UN-approved drums, 10–12 MT net weight per 20' FCL. |
| Shipping | 3-Bromo-5-Hydroxymethylpyridine is shipped in tightly sealed containers, protected from light and moisture. It is packaged according to chemical safety regulations, often with secondary containment. Shipping is typically by ground or certified hazardous material carriers, ensuring compliance with transport regulations for organic chemicals. Delivery includes proper labeling and documentation for traceability. |
| Storage | 3-Bromo-5-Hydroxymethylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep it away from incompatible substances such as oxidizing agents and strong acids. Store at room temperature and avoid moisture exposure. Properly label the container and ensure it is kept in a designated chemical storage cabinet. |
| Shelf Life | 3-Bromo-5-Hydroxymethylpyridine typically has a shelf life of 2 years when stored in a cool, dry, well-sealed container. |
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Purity 98%: 3-Bromo-5-Hydroxymethylpyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product purity. Melting Point 115°C: 3-Bromo-5-Hydroxymethylpyridine with a melting point of 115°C is used in fine chemical formulation, where it allows reliable solid handling and process control. Molecular Weight 188.03 g/mol: 3-Bromo-5-Hydroxymethylpyridine at a molecular weight of 188.03 g/mol is used in agrochemical development, where accurate dosing and formulation consistency are achieved. Stability Temperature up to 60°C: 3-Bromo-5-Hydroxymethylpyridine stable up to 60°C is used in storage and transport of research chemicals, where chemical integrity is maintained during material handling. Particle Size <20 µm: 3-Bromo-5-Hydroxymethylpyridine with particle size less than 20 µm is used in catalyst precursor manufacturing, where enhanced reactivity and dispersion are obtained. |
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In the realm of organic synthesis, specialty chemicals sometimes make all the difference. 3-Bromo-5-Hydroxymethylpyridine isn’t one of those household names, but anyone who spends time in complex molecule labs or the pharmaceutical industry knows just how valuable a versatile intermediate like this can be. Having spent years working in chemical research, I’ve witnessed how the right building blocks can speed up workflows, support rigorous quality requirements, and open avenues for innovation that simply weren’t practical a decade ago.
3-Bromo-5-Hydroxymethylpyridine brings a unique combination of bromine reactivity and a hydroxymethyl handle attached directly to a pyridine ring. The official chemical formula tells the story: C6H6BrNO, with a molecular weight just over 188 g/mol. The product typically arrives as an off-white to pale yellow solid—an appearance that makes it easy to recognize among the sea of powdered and crystalline reagents populating modern chemistry labs.
Purity matters, especially for tasks like medicinal chemistry or sensitive analytical work. Most reliable suppliers deliver this compound with a purity above 97%, usually verified by both HPLC and NMR. Water content runs low, so you avoid complications in reactions that can't tolerate moisture. As someone who’s faced project delays waiting for proper drying agents, I appreciate these guaranteed specs—it keeps experiments running on schedule and supports reproducible results.
This molecule steps in whenever researchers want to introduce a bromine atom into a heterocyclic scaffold or add functional diversity from a hydroxymethyl group. Anyone involved in developing new lead compounds for pharmaceuticals or exploring advanced agrochemical pathways benefits from its reactivity: that bromine at the 3-position makes cross-coupling chemistry straightforward, from Suzuki-Miyaura to Buchwald-Hartwig reactions. The hydroxymethyl group at the 5-position tacks on extra synthetic options, serving as a springboard for further modifications—think oxidations, substitutions, or protective group strategies.
In the field, chemists use this compound as an intermediate while building more intricate molecules with bioactive potential. The electronegative bromine atom makes the ring a bit more reactive, which opens up alternative synthetic routes. Having a precise molecular site for later transformation isn’t just a luxury; it’s a big part of why medicinal chemists keep coming back to this structure. Processes that used to call for lengthy protection and deprotection steps or involved difficult purification now run more smoothly.
Not all pyridine derivatives play the same role in synthesis. 3-Bromo-5-Hydroxymethylpyridine stands out thanks to two functional groups that provide flexibility. Basic 3-bromopyridine lacks the option to modify at the 5-position right off the bat—you’d have to bring in reagents or carefully orchestrate multi-step procedures just to insert a simple substituent. 5-Hydroxymethylpyridine, on its own, leaves you without the benefits of a good leaving group ready for substitution. Combining both groups into one molecule saves time, trims down waste, and helps teams reach their research milestones faster.
I’ve also noticed major practical advantages when working with this compound. Yields after coupling reactions come out reliably high, and impurities don’t build up to the point of jeopardizing downstream applications. In some university and contract research settings, budget is tight and time is even tighter; compounds with greater functional density can mean fewer purchase orders and less shelf space taken up by single-function materials. From my experience, it’s more than just a convenience — it can be the pivot that keeps projects on track for grants, regulatory submissions, or early-stage product launches.
3-Bromo-5-Hydroxymethylpyridine has proven especially valuable in the development of small-molecule drug candidates. Most new therapeutics demand structures that are both novel and synthetically accessible; this compound provides a launch pad for creating molecules that hit those marks. For instance, introducing heteroaromatic scaffolds with diverse side chains has fueled generations of kinase inhibitors, neurological drugs, and anti-infective agents. Having an intermediate with pre-installed points for both nucleophilic substitution and reductive amination takes some of the guesswork out of early-stage development.
It’s not just academia—industry relies on this class of intermediates as well. From my time consulting on contract manufacturing projects, I’ve seen how the ability to quickly iterate through analogs using a robust starting material can set one company apart from the rest. Turnaround times for lead optimization shrink noticeably when chemists can bypass lengthy route scouting. Teams spending less time trouble-shooting side reactions translates into clear cost savings and fewer last-minute headaches.
Working with halogenated pyridines comes with specific safety and reactivity considerations. For all its benefits, 3-Bromo-5-Hydroxymethylpyridine calls for careful management in handling and storage. Low moisture environments and well-sealed containers ensure stability, while routine use of gloves and protective eyewear minimize exposure risks. These sound like basic precautions, but overlooking them causes issues ranging from failed reactions to unwanted byproducts. I’ve learned, sometimes the hard way, the value of clear protocols and regular training for even the most seasoned team members.
Waste management matters too, especially since residues containing bromine tend to require specialized disposal. Corporate responsibility in the chemical sector doesn’t stop at product delivery—sound environmental practices trace back to responsible laboratory management. Many organizations now run robust waste segregation programs and work with licensed handlers for hazardous byproducts. Growing up in an era of increasing scrutiny over chemical footprints, it’s reassuring to see sustainable practices becoming part of normal lab routines. While not every challenge disappears, a culture of safety and stewardship sets the right tone for long-term research efforts.
A chemical’s true value shows up not just in its structure, but in the doors it opens. 3-Bromo-5-Hydroxymethylpyridine isn’t going to make headlines in consumer markets, yet its fingerprints appear on dozens of breakthrough discoveries each year. Think of teams synthesizing new anti-cancer candidates, fighting for lower drug resistance, or engineering plant protection agents: somewhere along the line, a versatile intermediate like this sits quietly at the foundation of those advances.
What sets this molecule apart in daily lab work is how much creative freedom it gives scientists. The push for more complex, targeted drugs means every functional group and ring substitution matters. By providing a bridge to both cross-coupling pathways and tailored functionalization, the compound allows researchers to move quickly from raw idea to tangible molecule. For start-ups and universities, fast progress makes a tangible difference in funding and publication chances.
As research into novel therapeutics and more sustainable chemicals ramps up, demand for adaptable intermediates heads in one direction—up. Better access to building blocks like 3-Bromo-5-Hydroxymethylpyridine means researchers spend less time on custom syntheses and more time refining ideas, testing hypotheses, and delivering next-generation products. Over the last decade, this shift has fueled a culture of fast prototyping and rapid iteration, especially in organizations looking to squeeze the most from tight budgets and timelines.
In my time collaborating with both process developers and academic groups, I’ve watched supply chains become more agile thanks to compounds with built-in flexibility. Where teams once scheduled weeks of intermediate preparation, many now shift their focus to late-stage diversification and functional tuning. This ability to tweak scaffolds on demand reduces the bottleneck that used to plague chemical discovery, leading to faster cycles of feedback between synthesis and bioactivity screening.
Finding a trustworthy supplier makes as much impact as the structure itself. Quality, consistency, and transparency stand out as top priorities. Most experienced researchers rely on suppliers with clear documentation, up-to-date certificates of analysis, and prompt technical support. It’s not unusual to hear colleagues swap stories about batches that failed to meet spec—one missed impurity peak, and whole projects get set back or scrapped. This lived experience underscores the need to partner with companies that take quality control seriously.
I’ve seen purchasing teams weigh not just price, but supply reliability, available lot sizes, and lead times. Supply chain disruptions—whether from global events or transportation mishaps—can throw wrenches into even the best project plans. Experts stress the importance of securing enough product for both screening and scale-up, along with keeping solid lines of communication open with suppliers. For teams expecting regulatory scrutiny, full traceability from order to delivery reduces risk and builds stakeholder confidence.
The chemical landscape never stands still. Increasing expectations around purity, reproducibility, and compliance drive continued adaptation in specialty chemicals. 3-Bromo-5-Hydroxymethylpyridine fits into this evolving world by offering dependable quality out of the box, so researchers can focus on end goals instead of troubleshooting the basics. As automation and data-driven design become more prevalent, compounds that respond predictably to a wide range of transformations carry even greater value.
Environmental standards grow stricter year by year. Professionals in the field recognize that even product intermediates need to live up to higher benchmarks, from clean manufacturing processes to minimized hazardous residues. Having access to a reagent that arrives with good documentation, low moisture, and minimal side contaminants checks off several regulatory boxes before a single experiment hits the bench. These details matter not just for compliance, but for smooth collaboration across global teams and facilities—from initial R&D phases to late-stage clinical production.
Not long ago, accessing molecules with precise substitution patterns required extended, multi-step procedures. Long reaction sequences ate into budgets and opened opportunities for errors that set projects back months. Tools like 3-Bromo-5-Hydroxymethylpyridine have changed this equation. By providing reliable starting points, chemists can now design more direct synthetic routes with far fewer purification headaches.
Even small differences in starting material availability or ease of use ripple out quickly in project planning. Analytical teams appreciate that clean, well-characterized intermediates produce less noisy data, allowing for faster progress during quality checks. Operations staff, for their part, benefit from solid physical handling properties and reliable batch-to-batch uniformity, which streamlines documentation. Across multiple roles, the less time spent firefighting synthesis challenges, the better outcomes for research and downstream applications.
While the pharmaceutical sector remains the main stage for this compound, its features fit equally well in the world of specialty materials and agricultural innovation. New pesticides, plant growth regulators, and small-molecule sensors all draw on heteroaromatic intermediates for their development. The ability to introduce both polarity and reactive side chains expands the toolkit available to synthetic chemists tackling emerging problems in food security and environmental monitoring.
My experience with materials science teams suggests cross-industry learning often drives surprising breakthroughs. For instance, molecular scaffolds originally developed for drug development later find use in the creation of novel electronic materials or advanced coatings. Access to adaptable intermediates speeds up this cross-pollination, supporting creativity and pragmatic problem solving across borders and industries.
No reagent or building block is free from issues, and every team faces roadblocks at some stage. For 3-Bromo-5-Hydroxymethylpyridine, challenges like scaling synthesis safely and economically, minimizing hazardous waste, and meeting ever-changing regulatory requirements sit front and center. Chemists who’ve spent time in both academic and industry labs know that small lapses in process control quickly escalate into bigger problems—so preventive planning always pays dividends.
Routine monitoring of impurities at each stage, robust process validation, and clear batch records help solve many recurring problems. Leaner, greener synthetic routes—utilizing milder reagents and energy-saving conditions—minimize both waste and costly reprocessing. Process engineers working with this compound have started leaning into continuous flow chemistry, which manages heat and hazardous intermediates more effectively. Continuous improvement, open training, and interdepartmental feedback keep everybody ahead of the curve. These proactive habits set a high bar for both product safety and workplace morale.
My time in research has taught me that real progress doesn’t usually hinge on breakthroughs alone, but on a steady stream of small, strategic advantages. Compounds like 3-Bromo-5-Hydroxymethylpyridine show how incremental gains—better yields, more reliable modifications, less time wasted—add up to long-term advances in science and industry. The right intermediate puts sophisticated tools into the hands of skilled researchers; creative problem-solvers make the most of what’s available to them.
Down the road, demand for adaptable, high-purity intermediates will only climb. Teams investing early in compounds that integrate smoothly with their synthesis ambitions end up with a competitive edge. Having spent years seeing projects blossom, stall, then surge ahead again based on access to the right building blocks, I’m convinced that reliable intermediates turn big goals into achievable milestones.
3-Bromo-5-Hydroxymethylpyridine serves as both a testament to progress made and a signal for what’s coming next. If the creativity of the global chemistry community says anything, this compound has a long future as an unsung hero behind many breakthrough discoveries. As expectations around speed, safety, and performance continue to grow, tools like this enable chemists to ask bolder questions—and get clearer, more rapid answers. The right molecule at the right time doesn’t just unlock reactions; it unlocks progress on challenges that matter to researchers, industry partners, and society at large.